Back to home
BD Interlink Injection Site
No active recall
Manufacturer: BD · FDA product code: FOZ · Category: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Severity Snapshot
144 total reports1993-12 – 2006-12 date range0% physician / facility reported100% manufacturer reported1 SKU variants
Failure & Consequence Profiles
Top Failure Modes
Click any bar to view those reports ↓
Top Patient Outcomes
Click any bar to view those reports ↓
Reporting Trend
Annual Reporting Volume
Click any bar to view those reports ↓
Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
Filter by failure mode
Filter by outcome
Loading reports…